US4666710A - Anti-perspirant compositions - Google Patents

Anti-perspirant compositions Download PDF

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Publication number
US4666710A
US4666710A US06/121,174 US12117480A US4666710A US 4666710 A US4666710 A US 4666710A US 12117480 A US12117480 A US 12117480A US 4666710 A US4666710 A US 4666710A
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United States
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weight
perspirant
compositions
aluminium
ethanol
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Expired - Lifetime
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US06/121,174
Inventor
Roy J. Clarkson
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Beecham Group PLC
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Beecham Group PLC
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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00Anti-perspirants or body deodorants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26Aluminium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/28Zirconium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof

Definitions

  • This invention relates to anti-perspirant compositions.
  • a desirable property of anti-perspirant compositions is that they should dry quickly after application to the skin.
  • the inclusion of a volatile solvent in the composition may often achieve this effect, the solvent evaporating quickly after application to leave a dry deposit of the active anti-perspirant material on the skin.
  • Ethanol has often been used for this purpose, since it is readily available and relatively non-toxic.
  • the use of high concentrations of ethanol can seriously reduce the efficacy of certain anti-perspirant compositions. This is particularly marked in the case of compositions containing an astringent anti-perspirant such as aluminium chlorhydrate.
  • this invention provides an aqueous anti-perspirant composition
  • an aqueous anti-perspirant composition comprising from 2 to 30% by weight of an astringent aluminium or zirconium salt as anti-perspirant agent, from 30 to 80% by weight of ethanol, and from 0.1 to 6% by weight of one or more C 14-18 fatty acids.
  • Anti-perspirant agents suitable for use with the composition include aluminium basic chloride, bromide or iodide, zirconyl hydroxychloride, and astringent aluminium/zirconium complexes such as aluminium zirconium chlorohydrates.
  • aluminium basic chloride means a compound having the approximate empirical formula Al 2 (OH).sub.(6-x) Cl x , where x is a number from 1 to 5.
  • x is a number from 1 to 5.
  • bromide and iodide have analogous formulae.
  • compositions of the invention contain from 0.5 to 4%, or more preferably 1.0 to 3% by weight of one or more C 14-18 fatty acids.
  • Suitable fatty acids include myristic, palmitic, stearic and iso-stearic acids, and mixtures thereof.
  • the most highly preferred fatty acids are myristic and palmitic acids.
  • compositions of the invention will normally contain from 5 to 20% by weight of anti-perspirant agent.
  • the preferred anti-perspirant agent for use in the compositions of the invention is an aluminium basic chloride wherein the atomic ratio of aluminium to chloride is from 1.9:1 to 2.1:1. This material is generally known as aluminium chlorhydrate.
  • compositions may contain further ingredients if desired, such as perfume, which will be present at conventional levels, such as 0.5 to 1% by weight.
  • compositions of the invention are more effective anti-perspirants than analogous compositions without fatty acids.
  • compositions will generally be adapted for application from a roll-ball or spray applicator.
  • Metal containers such as those used for aerosol compositions, are generally unsuitable for use with the present compositions since they may be subject to corrosion. Glass or plastic containers are therefore preferred.
  • compositions adapted for application from a roll-ball applicator will generally be thickened, for example, by the addition of conventional thickening agents, such as hydroxypropyl cellulose, or other thickening agents well known to those skilled in the art of formulating cosmetic compositions.
  • thickening agent such as hydroxypropyl cellulose, or other thickening agents well known to those skilled in the art of formulating cosmetic compositions.
  • hydroxypropyl cellulose When hydroxypropyl cellulose is used as thickening agent, it will generally be present in the composition in an amount from 0.1 to 2% by weight, more usually 0.1 to 1% or 0.3 to 0.8% by weight.
  • compositions may also be adapted for application from spray applicators, such as pump-sprays or squeeze-bottles.
  • compositions of the invention may be prepared as follows:
  • the myristic acid was dissolved in the ethanol with stirring, and then the aluminium chlorhydrate solution was added, and the mixture was stirred thoroughly.
  • the myristic acid was dissolved with stirring in the ethanol, followed by Klucel H, and then the aluminium chlorhydrate solution was added. The mixture was thoroughly stirred, to produce a composition suitable for application to the skin from a roll-ball applicator.
  • Example 2 Using the method described in Example 1, three compositions having the above constitution were prepared.
  • the fatty acids used were myristic, palmitic and isostearic acids.
  • compositions and a corresponding composition containing no fatty acid were tested on 20 subjects using the back screening method descrived in J. Soc. Cosmet. Chem. 29, 413-422 (1978).
  • compositions analogous to those in Examples 1 and 3 but having Crosterene S4310, a mixture of fatty acids, C 16 and C 18 acids predominating (Croda Chemicals Ltd.) was prepared and tested on 8 subjects using the back screening test, together with a corresponding composition containing no fatty acid.
  • the compositions produced mean sweat reductions of 46% and 17%, respectively.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Cosmetics (AREA)
  • Medicinal Preparation (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

An anti-perspirant composition includes 30% by weight of an anti-perspirant agent, aluminium chlorhydrate, 68.5% by weight of ethanol and 1.5% by weight of a long chain fatty acid, myristic acid.
The presence of the fatty acid counteracts the reduction in efficacy caused by the high concentration of ethanol.

Description

This invention relates to anti-perspirant compositions.
A desirable property of anti-perspirant compositions is that they should dry quickly after application to the skin. The inclusion of a volatile solvent in the composition may often achieve this effect, the solvent evaporating quickly after application to leave a dry deposit of the active anti-perspirant material on the skin. Ethanol has often been used for this purpose, since it is readily available and relatively non-toxic. However, the use of high concentrations of ethanol can seriously reduce the efficacy of certain anti-perspirant compositions. This is particularly marked in the case of compositions containing an astringent anti-perspirant such as aluminium chlorhydrate.
It is an object of the present invention to provide aqueous anti-perspirant compositions which contain relatively high levels of ethanol to promote quick drying after application to the skin, and which have good levels of anti-perspirant efficacy.
We have discovered that the reduction in efficacy caused by the presence of high concentrations of ethanol may be counteracted by the addition of certain fatty acids.
The addition of, inter alia, fatty acids to anti-perspirant compositions containing "Rehydrol" (a complex of aluminium chlorhydrate and propylene glycol) has been suggested. This is to counteract gelling of the compositions, which can occur with "Rehydrol". Gelling is not normally a problem with aqueous aluminium chlorhydrate compositions, so there has been no suggestion that the addition of fatty acids to aqueous aluminium chlorhydrate compositions would have any beneficial effects.
Accordingly, this invention provides an aqueous anti-perspirant composition comprising from 2 to 30% by weight of an astringent aluminium or zirconium salt as anti-perspirant agent, from 30 to 80% by weight of ethanol, and from 0.1 to 6% by weight of one or more C14-18 fatty acids.
Anti-perspirant agents suitable for use with the composition include aluminium basic chloride, bromide or iodide, zirconyl hydroxychloride, and astringent aluminium/zirconium complexes such as aluminium zirconium chlorohydrates.
When used herein, "aluminium basic chloride" means a compound having the approximate empirical formula Al2 (OH).sub.(6-x) Clx, where x is a number from 1 to 5. The corresponding bromide and iodide have analogous formulae.
Preferably, the compositions of the invention contain from 0.5 to 4%, or more preferably 1.0 to 3% by weight of one or more C14-18 fatty acids.
Suitable fatty acids include myristic, palmitic, stearic and iso-stearic acids, and mixtures thereof. The most highly preferred fatty acids are myristic and palmitic acids.
The compositions of the invention will normally contain from 5 to 20% by weight of anti-perspirant agent.
The preferred anti-perspirant agent for use in the compositions of the invention is an aluminium basic chloride wherein the atomic ratio of aluminium to chloride is from 1.9:1 to 2.1:1. This material is generally known as aluminium chlorhydrate.
The compositions may contain further ingredients if desired, such as perfume, which will be present at conventional levels, such as 0.5 to 1% by weight.
The compositions of the invention are more effective anti-perspirants than analogous compositions without fatty acids.
The compositions will generally be adapted for application from a roll-ball or spray applicator. Metal containers, such as those used for aerosol compositions, are generally unsuitable for use with the present compositions since they may be subject to corrosion. Glass or plastic containers are therefore preferred.
Compositions adapted for application from a roll-ball applicator will generally be thickened, for example, by the addition of conventional thickening agents, such as hydroxypropyl cellulose, or other thickening agents well known to those skilled in the art of formulating cosmetic compositions. When hydroxypropyl cellulose is used as thickening agent, it will generally be present in the composition in an amount from 0.1 to 2% by weight, more usually 0.1 to 1% or 0.3 to 0.8% by weight.
The compositions may also be adapted for application from spray applicators, such as pump-sprays or squeeze-bottles.
The compositions of the invention may be prepared as follows:
Dissolve the fatty acid(s) in the alcohol with stirring, and then add the thickener (if required) and stir until dissolved. Finally, add an aqueous solution of the anti-perspirant agent and stir thoroughly. Perfume may be added to the composition before adding the anti-perspirant agent.
The following Examples illustrate the invention:
EXAMPLE 1
______________________________________                                    
                % by weight                                               
______________________________________                                    
Myristic acid      1.5                                                    
Denatured ethanol 68.5                                                    
Aluminium chlorhydrate                                                    
                  30.0                                                    
(50% aqueous solution)                                                    
______________________________________                                    
The myristic acid was dissolved in the ethanol with stirring, and then the aluminium chlorhydrate solution was added, and the mixture was stirred thoroughly.
In the axilla screening test described in J. Soc. Cosmet. Chem. 29, 413-422 (1978), this composition produced a 43% sweat reduction compared with a 32% reduction for a corresponding composition containing no myristic acid and with 70% ethanol. (Significantly different at 0.02% level in Wilcoxon Matched Pairs Test).
EXAMPLE 2
______________________________________                                    
                % by weight                                               
______________________________________                                    
Myristic Acid     1.5                                                     
Denatured ethanol 67.84                                                   
Klucel H*         0.66                                                    
Aluminium chlorhydrate                                                    
                  30.00                                                   
(50% aqueous solution)                                                    
______________________________________                                    
 *Klucel H is hydroxypropyl cellulose (Hercules Powder Co.).              
The myristic acid was dissolved with stirring in the ethanol, followed by Klucel H, and then the aluminium chlorhydrate solution was added. The mixture was thoroughly stirred, to produce a composition suitable for application to the skin from a roll-ball applicator.
EXAMPLE 3
______________________________________                                    
                 % by weight                                              
______________________________________                                    
Fatty Acid          1.5                                                   
Aluminium Chlorhydrate                                                    
                   30.0                                                   
(5O% aqueous solution)                                                    
Denatured ethanol  68.5                                                   
______________________________________                                    
Using the method described in Example 1, three compositions having the above constitution were prepared. The fatty acids used were myristic, palmitic and isostearic acids.
These compositions and a corresponding composition containing no fatty acid were tested on 20 subjects using the back screening method descrived in J. Soc. Cosmet. Chem. 29, 413-422 (1978).
The results are shown below.
______________________________________                                    
Fatty Acid  Mean % Sweat Reduction                                        
______________________________________                                    
 --         34                                                            
Myristic    54                                                            
Palmitic    54                                                            
Isostearic  39                                                            
______________________________________                                    
EXAMPLE 4
A composition analogous to those in Examples 1 and 3 but having Crosterene S4310, a mixture of fatty acids, C16 and C18 acids predominating (Croda Chemicals Ltd.) was prepared and tested on 8 subjects using the back screening test, together with a corresponding composition containing no fatty acid. The compositions produced mean sweat reductions of 46% and 17%, respectively.

Claims (7)

I claim:
1. An aqueous anti-perspirant composition, consisting essentially of from 2 to 30% by weight of an astringent aluminium or zirconium salt as anti-perspirant agent, from 30 to 80% by weight of ethanol, from 0.16 to 6% by weight of one or more C14-18 fatty acids, and water.
2. A composition according to claim 1, wherein the anti-perspirant agent comprises aluminium basic chloride, bromide, or iodide, zirconyl hydroxychloride, or an aluminium zirconium chlorohydrate.
3. A composition according to claim 1, wherein from 1.0 to 3% by weight of one or more C14-18 fatty acids is present.
4. A composition according to claim 1, wherein the fatty acid is myristic, palmitic, stearic, or iso-stearic acid, or a mixture of any thereof.
5. A composition according to claim 1, wherein from 5 20% by weight of said anti-perspirant agent is present.
6. An aqueous anti-perspirant composition, consisting essentially of from 2 to 30% by weight of an astringent aluminium or zirconium salt as anti-perspirant agent, from 30 to 80% by weight of ethanol, from 0.16 to 6% by weight of one or more C14-18 fatty acids, and water and a thickener.
7. An aqueous anti-perspirant composition consisting essentially of from 2 to 30% by weight of an astringent aluminium or zirconium salt as anti-perspirant agent, from 30 to 80% by weight of ethanol, from 0.16 to 6% by weight of one or more C14-18 fatty acids, and water and a perfume.
US06/121,174 1979-02-22 1980-02-13 Anti-perspirant compositions Expired - Lifetime US4666710A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB7906281 1979-02-22
GB7906281 1979-02-22

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US4666710A true US4666710A (en) 1987-05-19

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US (1) US4666710A (en)
EP (1) EP0016533B1 (en)
JP (1) JPS55115817A (en)
AU (1) AU534751B2 (en)
CA (1) CA1127540A (en)
DE (1) DE3070638D1 (en)
DK (1) DK70780A (en)
GB (1) GB2043445B (en)
IE (1) IE49271B1 (en)
ZA (1) ZA80882B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995031961A1 (en) * 1994-05-25 1995-11-30 The Procter & Gamble Company Gel stick compositions comprising optically enriched gellants

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3147136A (en) * 1961-01-11 1964-09-01 Owens Illinois Glass Co Process for forming a grit-blasted and methyl methacrylate-epoxy resin coated glass surface
GB8518081D0 (en) * 1985-07-17 1985-08-21 Beecham Group Plc Compositions
DK483587D0 (en) * 1987-09-15 1987-09-15 Riemann & Co Aps Claus ANTIPERSPIRANT PREPARATION
GB9604341D0 (en) * 1996-02-29 1996-05-01 Unilever Plc Antiperspirant composition
JP6180995B2 (en) * 2014-05-27 2017-08-16 ライオン株式会社 Antiperspirant composition

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB480379A (en) * 1936-10-29 1938-02-22 William Cabler Moore A new and useful composition as a deodorant and for application to the human skin
GB1267959A (en) * 1968-10-23 1972-03-22 Armour Pharma Method of making alcohol-soluble complexes of aluminum
GB1319437A (en) * 1970-11-09 1973-06-06 Armour Pharma Basic aluminium bromide compositions
US4053581A (en) * 1975-08-15 1977-10-11 Lever Brothers Company Antiperspirant solution containing a mixture of substantially volatile and substantially non-volatile siloxane liquids
US4152416A (en) * 1976-09-17 1979-05-01 Marra Dorothea C Aerosol antiperspirant compositions delivering astringent salt with low mistiness and dustiness
US4174386A (en) * 1975-03-03 1979-11-13 Marra Dorothea C Aerosol antiperspirant compositions with good adherence to the skin

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU484620B2 (en) * 1973-10-26 1975-05-01 Armour Pharmaceutical Company Zinc and zirconium complexes of basic aluminum halides and methods of making same
JPS5470436A (en) * 1977-11-15 1979-06-06 Lion Dentifrice Co Ltd Antiisweat agent

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB480379A (en) * 1936-10-29 1938-02-22 William Cabler Moore A new and useful composition as a deodorant and for application to the human skin
GB1267959A (en) * 1968-10-23 1972-03-22 Armour Pharma Method of making alcohol-soluble complexes of aluminum
GB1319437A (en) * 1970-11-09 1973-06-06 Armour Pharma Basic aluminium bromide compositions
US4174386A (en) * 1975-03-03 1979-11-13 Marra Dorothea C Aerosol antiperspirant compositions with good adherence to the skin
US4053581A (en) * 1975-08-15 1977-10-11 Lever Brothers Company Antiperspirant solution containing a mixture of substantially volatile and substantially non-volatile siloxane liquids
US4152416A (en) * 1976-09-17 1979-05-01 Marra Dorothea C Aerosol antiperspirant compositions delivering astringent salt with low mistiness and dustiness

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Ash et al., A Formulary of Cosmetic Preparations, 1977, pp. 7, 8, 9, 10 to 14, & 20 to 24. *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995031961A1 (en) * 1994-05-25 1995-11-30 The Procter & Gamble Company Gel stick compositions comprising optically enriched gellants
US5552136A (en) * 1994-05-25 1996-09-03 The Procter & Gamble Company Gel stick compositions comprising optically enriched gellants

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DE3070638D1 (en) 1985-06-20
IE800344L (en) 1980-08-22
EP0016533A3 (en) 1981-08-26
GB2043445B (en) 1983-08-17
CA1127540A (en) 1982-07-13
IE49271B1 (en) 1985-09-04
GB2043445A (en) 1980-10-08
ZA80882B (en) 1981-02-25
AU534751B2 (en) 1984-02-16
EP0016533B1 (en) 1985-05-15
EP0016533A2 (en) 1980-10-01
DK70780A (en) 1980-08-23
AU5540880A (en) 1980-08-28
JPS55115817A (en) 1980-09-06

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